Canonical Allele Identifier: PA2741980252
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2868475
ClinVar RCV Id: RCV003646756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ile858Thr
CA376556672
NM_020975.6:c.2573T>C